Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000151 | ubiquitin ligase complex | 3 | 1 |
GO:0005634 | nucleus | 5 | 1 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: E9AVB4
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 1 |
GO:0005488 | binding | 1 | 2 |
GO:0005515 | protein binding | 2 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 1 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 1 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 1 |
GO:0097602 | cullin family protein binding | 3 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
GO:0008270 | zinc ion binding | 6 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
GO:0046914 | transition metal ion binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.499 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.670 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.443 |
DEG_SPOP_SBC_1 | 123 | 127 | PF00917 | 0.526 |
DOC_CDC14_PxL_1 | 69 | 77 | PF14671 | 0.752 |
DOC_CYCLIN_yCln2_LP_2 | 116 | 122 | PF00134 | 0.720 |
DOC_PP4_FxxP_1 | 192 | 195 | PF00568 | 0.484 |
DOC_PP4_FxxP_1 | 247 | 250 | PF00568 | 0.299 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.816 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.750 |
DOC_USP7_MATH_2 | 102 | 108 | PF00917 | 0.758 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.785 |
DOC_WW_Pin1_4 | 173 | 178 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.751 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.779 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.712 |
LIG_14-3-3_CanoR_1 | 254 | 259 | PF00244 | 0.513 |
LIG_BIR_III_4 | 36 | 40 | PF00653 | 0.576 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.676 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.728 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.748 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.530 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.438 |
LIG_LIR_Apic_2 | 190 | 195 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 107 | 116 | PF02991 | 0.627 |
LIG_LIR_Nem_3 | 107 | 112 | PF02991 | 0.630 |
LIG_LIR_Nem_3 | 49 | 55 | PF02991 | 0.634 |
LIG_NRBOX | 74 | 80 | PF00104 | 0.689 |
LIG_Pex14_2 | 2 | 6 | PF04695 | 0.648 |
LIG_SH2_CRK | 261 | 265 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.411 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.598 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.710 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.713 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.641 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.719 |
LIG_SUMO_SIM_par_1 | 74 | 83 | PF11976 | 0.771 |
LIG_TRAF2_1 | 101 | 104 | PF00917 | 0.748 |
LIG_WRC_WIRS_1 | 106 | 111 | PF05994 | 0.673 |
LIG_WW_2 | 195 | 198 | PF00397 | 0.466 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.706 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.756 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.768 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.661 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.597 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.705 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.622 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.711 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.672 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.513 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.725 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.743 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.720 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.671 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.644 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.670 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.758 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.660 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.645 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.589 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.660 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.530 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.521 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.707 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.594 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.559 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.599 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.684 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.639 |
MOD_PIKK_1 | 196 | 202 | PF00454 | 0.700 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.659 |
MOD_Plk_1 | 134 | 140 | PF00069 | 0.656 |
MOD_Plk_2-3 | 234 | 240 | PF00069 | 0.513 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.679 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.484 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.744 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.625 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.782 |
MOD_ProDKin_1 | 173 | 179 | PF00069 | 0.555 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.468 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.752 |
MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.487 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.781 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.711 |
MOD_SUMO_rev_2 | 178 | 188 | PF00179 | 0.548 |
MOD_SUMO_rev_2 | 230 | 238 | PF00179 | 0.513 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3K6 | Leptomonas seymouri | 37% | 94% |
A0A3S7WWM2 | Leishmania donovani | 85% | 99% |
A4HBY6 | Leishmania braziliensis | 67% | 100% |
A4HZC7 | Leishmania infantum | 84% | 99% |
Q4QC66 | Leishmania major | 84% | 100% |